US20200061247A1 - A biomimetic artificial blood vessel and a production method thereof - Google Patents
A biomimetic artificial blood vessel and a production method thereof Download PDFInfo
- Publication number
- US20200061247A1 US20200061247A1 US16/612,677 US201816612677A US2020061247A1 US 20200061247 A1 US20200061247 A1 US 20200061247A1 US 201816612677 A US201816612677 A US 201816612677A US 2020061247 A1 US2020061247 A1 US 2020061247A1
- Authority
- US
- United States
- Prior art keywords
- blood vessel
- artificial blood
- polycaprolactone
- ethyl cellulose
- production method
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 210000004204 blood vessel Anatomy 0.000 title claims abstract description 68
- 239000002473 artificial blood Substances 0.000 title claims abstract description 57
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 39
- 230000003592 biomimetic effect Effects 0.000 title claims abstract description 10
- 238000000034 method Methods 0.000 claims abstract description 30
- 238000001523 electrospinning Methods 0.000 claims abstract description 29
- 239000001856 Ethyl cellulose Substances 0.000 claims description 43
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 claims description 43
- 229920001249 ethyl cellulose Polymers 0.000 claims description 43
- 235000019325 ethyl cellulose Nutrition 0.000 claims description 43
- 229920001610 polycaprolactone Polymers 0.000 claims description 42
- 239000004632 polycaprolactone Substances 0.000 claims description 36
- 102000008186 Collagen Human genes 0.000 claims description 30
- 108010035532 Collagen Proteins 0.000 claims description 30
- 229920001436 collagen Polymers 0.000 claims description 30
- 239000000203 mixture Substances 0.000 claims description 24
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 20
- 239000002114 nanocomposite Substances 0.000 claims description 17
- 239000002121 nanofiber Substances 0.000 claims description 14
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 10
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 9
- 239000003960 organic solvent Substances 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 6
- 238000011282 treatment Methods 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 3
- 230000005611 electricity Effects 0.000 claims description 3
- 231100000053 low toxicity Toxicity 0.000 claims description 3
- 230000003068 static effect Effects 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- 230000000877 morphologic effect Effects 0.000 abstract description 2
- 239000000243 solution Substances 0.000 description 26
- 210000001519 tissue Anatomy 0.000 description 8
- 239000000835 fiber Substances 0.000 description 5
- 238000001727 in vivo Methods 0.000 description 5
- 206010053567 Coagulopathies Diseases 0.000 description 4
- 210000004027 cell Anatomy 0.000 description 4
- 230000035602 clotting Effects 0.000 description 4
- 229920001059 synthetic polymer Polymers 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 102000010834 Extracellular Matrix Proteins Human genes 0.000 description 3
- 108010037362 Extracellular Matrix Proteins Proteins 0.000 description 3
- 206010061218 Inflammation Diseases 0.000 description 3
- 238000010835 comparative analysis Methods 0.000 description 3
- 230000005802 health problem Effects 0.000 description 3
- 210000005003 heart tissue Anatomy 0.000 description 3
- 238000000338 in vitro Methods 0.000 description 3
- 230000004054 inflammatory process Effects 0.000 description 3
- 229920005615 natural polymer Polymers 0.000 description 3
- 239000011550 stock solution Substances 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 2
- 230000036772 blood pressure Effects 0.000 description 2
- 210000002808 connective tissue Anatomy 0.000 description 2
- 230000003013 cytotoxicity Effects 0.000 description 2
- 231100000135 cytotoxicity Toxicity 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000012456 homogeneous solution Substances 0.000 description 2
- 210000000987 immune system Anatomy 0.000 description 2
- 238000001361 intraarterial administration Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002105 nanoparticle Substances 0.000 description 2
- 230000001575 pathological effect Effects 0.000 description 2
- 230000035755 proliferation Effects 0.000 description 2
- 230000004936 stimulating effect Effects 0.000 description 2
- 230000008093 supporting effect Effects 0.000 description 2
- 239000002407 tissue scaffold Substances 0.000 description 2
- 208000024172 Cardiovascular disease Diseases 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000003679 aging effect Effects 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000000560 biocompatible material Substances 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 230000000747 cardiac effect Effects 0.000 description 1
- 208000015606 cardiovascular system disease Diseases 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007123 defense Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 210000002744 extracellular matrix Anatomy 0.000 description 1
- 210000003709 heart valve Anatomy 0.000 description 1
- 238000007914 intraventricular administration Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 210000004698 lymphocyte Anatomy 0.000 description 1
- 230000003278 mimic effect Effects 0.000 description 1
- 239000002062 molecular scaffold Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 208000037803 restenosis Diseases 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 210000000130 stem cell Anatomy 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/04—Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
- A61F2/06—Blood vessels
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/18—Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/20—Polysaccharides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/22—Polypeptides or derivatives thereof, e.g. degradation products
- A61L27/24—Collagen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/26—Mixtures of macromolecular compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L27/507—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials for artificial blood vessels
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D1/00—Treatment of filament-forming or like material
- D01D1/02—Preparation of spinning solutions
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/0007—Electro-spinning
- D01D5/0015—Electro-spinning characterised by the initial state of the material
- D01D5/003—Electro-spinning characterised by the initial state of the material the material being a polymer solution or dispersion
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/24—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2240/00—Manufacturing or designing of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2240/001—Designing or manufacturing processes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2400/00—Materials characterised by their function or physical properties
- A61L2400/12—Nanosized materials, e.g. nanofibres, nanoparticles, nanowires, nanotubes; Nanostructured surfaces
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2509/00—Medical; Hygiene
Abstract
A three-dimensional biomimetic artificial blood vessel that is biodegradable and biocompatible, is inspired by the morphological structure and physiological role of blood vessels having small diameter in the human circulatory system. A method of production by electro spinning is also disclosed.
Description
- This invention relates to a three-dimensional biomimetic artificial blood vessel that is biodegradable and biocompatible, inspired by the morphological structure and physiological role of blood vessels having small diameter in the human circulatory system, and the method of production by means of electrospinning.
- Cardiovascular system diseases are one of the leading health problems when examined in terms of mortality and morbidity rates worldwide. Studies in the field of tissue engineering in order to prevent or cure these kind of diseases have been promising.
- The blood vessels, which are important components of the circulatory system, can lose their function due to congestion or different health problems and can lead to major health problems by causing blood flow continuity interruption to the region. Although these modern therapies, which are often used today, based on the ability to remove intraventricular obstruction by mechanical means are life-saving, there is the possibility of restenosis, vessel narrowing or collapse and similar complications that occur after treatment. At the same time, due to high treatment costs, it creates an economic burden in the countries that allocate a share of treatment for circulatory system diseases for both individuals and health insurances.
- One of the most frequently methods used today comprise transfer of blood vessels having small diameters in an allogenic or autologous way. However, the difficulty of finding suitable donors and the possible rejection of tissue from the immune system limit the clinical practice of such treatments. For these reasons, production of blood vessels having a small diameter having mechanical properties suitable for their purpose of use with biocompatible materials hold a great deal of promise by means of modernizing present treatment methods and value added to patient's life. However, it is known that the materials produced for this purpose and the work done in this area have disadvantages of lacking essential features and requirements sought in an artificial blood vessel such as lack of biocompatibility, not preventing clotting, not having appropriate mechanical properties, not being suitable for long-term use.
- In the known state of the art, WO2013109642 discloses compositions comprising a nanofiber framework having a printed configuration that mimics a tissue structure such as heart tissue, which is fertilized with one or more related stem cells. The invention described in said document further discloses, methods for treating damaged heart tissue in a damaged heart by providing application of the composition in an effective amount to the damaged cardiac tissue. This document also describes methods for preparing nanofiber tissue scaffold compositions. Said tissue scaffold is obtained by electrospinning using biocompatible polycaprolactone polymer and also by attaching an extracellular matrix protein onto the nanofiber scaffold. In the said invention, collagen is used as extracellular matrix protein.
- In United States patent no. US2006204539, which is part of the state of the art, refers to compositions and methods for preparing electrospun matrices containing at least one natural biological material and at least one synthetic polymer material. The invention described in the document discloses that while the natural component matrices are highly biocompatible, the polymer component imparts an additional mechanical strength to the molecular weight scaffold and/or facilitates production by increasing the viscosity and bending properties of the solution during electrospinning. The object of the present invention is to obtain electrospun matrices for use in blood vessels, heart valves, vascular or cardiac structures. It is mentioned in said document that the electrospun nanofibers comprise polycaprolactone, collagen or cellulose derivatives.
- The object of this invention is to realize an artificial blood vessel which is suitable for use in the human body and which does not cause intra-arterial clotting, is composed of nano-sized fiber scaffold with high mechanical properties and elasticity against blood pressure, other external factors and aging effects and a production method thereof.
- Another object of the invention is to realize an artificial blood vessel having endothelization stimulating and supporting effect on the outer wall and production thereof with electrospinning technique.
- Another object of the invention is to realize an artificial blood vessel having a nanocomposite structure skeleton formed by superimposed nano-sized fibers made of natural and synthetic polymers and a method for production thereof.
- A “Biomimetic Artificial Blood Vessel and Production Method Thereof” to achieve the purpose of this invention is illustrated in the attached figures, wherein said figures disclose;
-
FIG. 1 : The SEM (Scanning Electron Microscope) image of the artificial blood vessel scaffold of the present invention. - (a) Image of an artificial blood vessel structure scaffold of the invention at magnification of 5.00 KX
- (b) Image of an artificial blood vessel structure scaffold of the invention at magnification of 20.00 KX
-
FIG. 2 : Fiber dimensions frequency graph of the artificial blood vessel scaffold of the present invention. -
FIG. 3 : The column charts showing the in-vitro cytotoxicity results measured for 24, 48 and 72 hours, respectively, according to the changing contents of biomimetic artificial veins. -
FIG. 4 : Comparative analysis photos of tissue response after pathological examinations performed after 6 weeks of in-vitro testing. - In collagen-free specimens;
- (a) At 20× magnification, the arrow indicates the thickest zone of inflammation.
- (b) At 40× magnification, upper arrow points to the giant cell and lower arrow points to plasma and lymphocyte cells that entered the lumen.
- (c) At 40× magnification, the arrow indicates proliferation of connective tissue.
- In collagen containing specimens;
- (d) At 20× magnification, the arrow indicates the thickest zone of inflammation.
- (e and f) are photos taken at 40× magnification.
-
FIG. 5 : The flow diagram of the production method for artificial blood vessel according to the invention. - The artificial blood vessel of the invention is suitable for use in the human body, it does not cause intra-arterial clotting and made up of nano composite structure scaffolds that has strong mechanical properties against blood pressure, outer effects and ageing and has strong elasticity. The artificial blood vessels of the invention are made up of the abovementioned nanocomposite structure and they have endothelization stimulating and supporting effect and they are biocompatible and biodegradable.
- To this end, the artificial blood vessel forming structure scaffold of the invention comprises Polycaprolactone (PCL), that is a synthetic polymer and which has strong mechanical properties and is suitable for use in electrospinning technique; Ethyl cellulose (EC), that is a natural polymer and which is biocompatible and has low toxicity; and
- Collagen, which is one of the building blocks of the extracellular matrix and thus imitating it and also provides cell accumulation of the structure scaffolds. The collagen structure also provides elasticity to the structure scaffold and contributes to biocompatibility and endothelization.
- According to present invention, a method for production of biomimetic artificial blood vessel (100) comprises the steps of
-
- Preparation of ethyl cellulose solution (101) at a certain concentration by dissolving biocompatible and low toxicity natural ethyl cellulose polymer in at least one organic solvent,
- Preparation of polycaprolactone solution (102) at a certain concentration by dissolving the synthetic polycaprolactone polymer in at least one organic solvent,
- Mixing the ethylcellulose solution and the polycaprolactone solution at a certain ratio (103)
- Addition of collagen dissolved in at least one organic solvent into the mixture comprising ethyl cellulose and polycaprolactone solution (104), at a certain ratio
- Stirring the mixture comprising ethyl cellulose, polycaprolactone and collagen to have a homogenous solution (105),
- Subjecting the homogenous solution comprising ethyl cellulose, polycaprolactone and collagen to the electrospinning process (106) for a while in an electrospinning machine that comprise at least one needle and a movable, cylindrical collector via adjusting parameters of voltage, distance between the needle and the collector and flow rate that effect the nanofiber diameter and morphology,
- Obtaining the hollow nano-composite structure scaffold (107) via subjecting the mixture to electrospinning (106) and then collecting the nanofibers formed by movement of the polymers with the static electricity to form nanofibers on the cylindrical collector,
- Obtaining of the artificial blood vessel (108) via drying of the obtained structure scaffold.
- In a preferred embodiment of the method for artificial blood vessel production (100) according to invention, the ethyl cellulose is dissolved in the organic solvent such that there is 1% of ethyl cellulose in the solution by weight. In order to obtain this, the ethyl cellulose solution (101) is prepared by addition of ethyl cellulose to a solution comprising dimethylacetamide (DMA) and tetrahydrofuran (THF) in a ratio of 60:40 by weight.
- In a preferred embodiment of the artificial blood vessel manufacturing method (100) of the invention, the polycaprolactone solution (102) is prepared by adding polycaprolactone polymer to the solvent preferably comprising dimethylacetamide (DMA) and tetrahydrofuran (THF) in a ratio of 60:40 by weight, in an amount of 10% by weight.
- After the preparation of both the ethyl cellulose solution (101) and the polycaprolactone solution (102), the solutions are then mixed at a ratio of 50:50 by weight (103).
- In the production method of the artificial blood vessel (100) according to present invention; after mixing of the ethyl cellulose solution with polycaprolactone solution (103) a solution of collagen, preferably dissolved in acetic acid, is added to the solution comprising ethyl cellulose and polycaprolactone, such that the mixture comprise 0.1% of collagen by weight (104). The resulting final mixture is mixed, preferably stirred on a magnetic stirrer, preferably for 10 minutes, to obtain a homogeneous solution (105).
- In the artificial blood vessel production method of the invention (100), after obtaining a homogenous solution (105), the obtained mixture is transferred to an injector and loaded to the pump section of an electrospinning machine, which leads to progression of a predetermined amount of polymer at a predetermined time interval. The flow rate of the mixture loaded in the electrospinning machine preferably has a value of 1.75 ml/h The voltage of the electricity that is then applied to provide the production of nanofibers is preferably about 36 kV. In the artificial blood vessel production method according to the invention (100), hollow nano-composite scaffolds are obtained in a cylindrical structure by collecting the nanofibers obtained by electrospinning (106) for 3 to 5 hours and collecting the electrospun fibers on a movable collector having a cylindrical structure. In said method (100), the electrospinning process (106) is preferably carried out for 4 hours. In the artificial blood vessel manufacturing method of the invention (100), in a preferred embodiment the diameter of the cylindrical structured collector used in the electrospinning process is 0.5 cm.
- In the artificial blood vessel manufacturing method (100) according to the present invention, the obtained nanocomposite scaffold is dried in a 23 to 50° C. oven for 3 to 8 hours to obtain an artificial blood vessel (108). In a preferred embodiment of the invention, the nano composite scaffold is dried for 4 hours at 35° C. in an oven. The obtained artificial blood vessel can be used by cutting the blood vessel at a certain length.
- Experimental studies carried out in order to achieve the object of the method (100) of the present invention aim to combine the different properties of polycaprolactone (PCL), ethyl cellulose (EC) and collagen in a single final product by means of electrospinning technique and, it is aimed to have as fine fiber dimensions as possible so that this final product should not be prone to clotting and would support cell attachment at the maximum level with help of the maximized surface area.
- In the method according to the invention, firstly a solvent stock solution is prepared by mixing dimethylacetamide (DMA) and tetrahydrofuran (THF) in a weight ratio of (60:40). Afterwards, polycaprolactone (PCL) was dissolved in this stock solution in a 10% weight ratio.
- In experimental studies to achieve the purpose of method of the invention (100), six different samples were prepared at different concentrations to compare the biocompatibility of the subject blood vessel with in vivo tests.
- For this purpose, three separate solutions were prepared at different concentrations, namely comprising 0.5%, 0.75% and 1.0% of ethyl cellulose (EC) by weight in the stock solution. Afterwards, into every solution comprising ethyl cellulose (EC), the solution comprising 10% by weight polycaprolactone has been added such that in the final mixture the solutions have a ratio of 50:50 by weight. Then each of the 3 separate samples obtained in this way were divided into two groups. Then one group of each sample was taken and an addition of collagen dissolved in acetic acid was added such that there will be 0.1% collagen in the final mixture. The final mixture was stirred for 10 minutes to obtain a homogeneous solution in the magnetic stirrer.
- The weight ratios of 6 different solutions obtained in this way are given in Table 1.
-
TABLE 1 The weight content of 6 different samples prepared are shown below. Group I Group II PCL EC PCL EC Collagen Sample I 10% 0.5% Sample II 10% 0.75 % Sample III 10% 1 % Sample IV 10% 0.5% 0.1 % Sample V 10% 0.75% 0.1 % Sample VI 10% 1% 0.1% - Each sample was then loaded into the precision digital pump of the electrospinning apparatus via a 10 ml plastic syringe and delivered into the electric field at a flow rate of 1.75 ml/hr. The voltage of the electric field is set at 36.5 kV. In the mean time, with these parameters the nanofiber structure scaffold starts to collect on the collector and the process of electrospinning was continued for 4 hours. After the end of the electrospinning process, the formed nano composite scaffold was left to stand at 35° C. for 4 hours to remove solvent residues. After the required characterization tests in vitro cytotoxicity results were measured for 24, 48, 72 hours in 6 different samples for biocompatibility assessments (
FIG. 2 ). - In accordance with the biocompatibility results given in
FIG. 2 , sample VI was selected for in vivo applications. For comparative analysis, Sample III which did not comprise collagen was used for in vivo applications. For this, said solutions were subjected to electrospinning process such that the obtained nanocomposite structure scaffold would form on a stainless steel collector having 0.5 cm diameter was used to obtain morphologically similar scaffolds. As a result of the electrospinning process, Nano composite scaffolds with a length of 12 cm and a weight of 6 g and an internal diameter of 0.5 cm were obtained. The obtained structure was prepared for in-vivo testing by separating the scaffold from the collector and keeping it hollow while maintaining the cylindrical structure. The blood vessels obtained from Example I III (collagen-free) and Example VI (with collagen) that are used for in-vivo studies are implanted into the animal without use of catheters etc. Finally, pathological examinations were performed and comparative analysis photographs of tissue responses are given inFIG. 4 . In the collagen-free sample, the reaction of the immune system, which is the response to the artificial blood vessel by the tissue, is observed. In the case of collagen-containing sample, it is observed that the artificial blood vessel demonstrates a high biocompatibility in the animal, so it does not lead to tissue proliferation, is not invaded by defense cells and a minimum of inflammation, which is the tissue response to foreign material is observed and formation of a protective pseudo-capsule adventitia around the artificial blood vessel of the living body was seen. This is the basis for endothelialization. - By the method of the invention (100), nanofibers are produced with synergies obtained by use of natural and synthetic polymers at specific ratios, and these nanofibers are overlaid to form a nanocomposite structure scaffold with the nano composite structure scaffold, biomimetic blood vessels which have small diameter compared known artificial blood vessels are produced and these mimic natural blood vessels morphologically and physiologically with high biocompatibility.
- Around this basic concepts, it is possible to develop a wide variety of applications for the invention subject matter “Biomimetic Artificial Blood Vessel and a Production Method (100) thereof” and the invention is not limited to the examples described herein, but is essentially as specified in the claims.
Claims (20)
1. A method for a production of biomimetic artificial blood vessel characterized in that said method comprises the steps of:
preparation of ethyl cellulose solution (101) at a certain concentration by dissolving biocompatible and low toxicity natural ethyl cellulose polymer in at least one organic solvent;
preparation of polycaprolactone solution (102) at a certain concentration by dissolving the synthetic polycaprolactone polymer in at least one organic solvent, Mixing the ethylcellulose solution and the polycaprolactone solution at a certain ratio (103);
addition of collagen dissolved in at least one organic solvent into the mixture comprising ethyl cellulose and polycaprolactone solution (104), at a certain ratio stirring the mixture comprising ethyl cellulose, polycaprolactone and collagen to have a homogenous solution (105);
subjecting the homogenous solution comprising ethyl cellulose, polycaprolactone and collagen to the electrospinning process (106) in an electrospinning machine that comprise at least one needle and a movable, cylindrical collector via adjusting parameters of voltage, distance between the needle and the collector and flow rate that effect the nanofiber diameter and morphology;
obtaining the hollow nano-composite structure scaffold (107) via subjecting the mixture to electrospinning (106) and then collecting the nano fibers formed by movement of the polymers with the static electricity to form nanofibers on the cylindrical collector; and
obtaining of the artificial blood vessel (108) via drying of the obtained structure scaffold.
2. An artificial blood vessel production method according to claim 1 , characterized in that the step (101) the ethyl cellulose is dissolved in the organic solvent such that there is 1% of ethyl cellulose in the solution by weight.
3. An artificial blood vessel production method according to claim 1 , characterized in that the ethyl cellulose solution is prepared by addition of ethyl cellulose to a solution comprising dimethylacetamide (DMA) and tetrahydrofuran (THF) in a ratio of 60:40 by weight.
4. An artificial blood vessel production method according to claim 1 , characterized in that in step (102) the polycaprolactone solution is prepared as a 10% by weight polycaprolactone polymer in the solvent.
5. An artificial blood vessel production method according to claim 1 , characterized in that in step (102) polycaprolactone solution is prepared by adding polycaprolactone polymer to the solvent comprising dimethylacetamide (DMA) and tetrahydrofuran (THF) in a ratio of 60:40 by weight.
6. An artificial blood vessel production method according to claim 1 , characterized in that in step (103) ethyl cellulose solution and the polycaprolactone solution is mixed by 50:50 by weight.
7. An artificial blood vessel production method according to claim 1 , characterized in that in step (104) collagen dissolved in acetic acid is added to ethyl cellulose and polycaprolactone solution.
8. An artificial blood vessel production method according to claim 1 , characterized in that in step (104) a solution of collagen is added to the solution comprising ethyl cellulose and polycaprolactone, such that the mixture comprise 0.1% of collagen by weight (104)
9. An artificial blood vessel production method according to claim 1 , characterized in that in step (105) a mixture comprising ethyl cellulose, polycaprolactone and collagen are mixed in a magnetic stirrer for 10 minutes.
10. An artificial blood vessel manufacturing method according to claim 1 , characterized in that the mixture comprising ethyl cellulose, polycaprolactone and collagen is transferred to an injector and loaded to the pump section of an electrospinning machine, which leads to progression of a predetermined amount of polymer at a predetermined time interval.
11. An artificial blood vessel production method according to claim 1 , characterized in that the mixture containing ethyl cellulose, polycaprolactone and collagen is subjected to electrospinning treatment at a flow rate of 1.75 ml/hr.
12. An artificial blood vessel production method according to claim 1 , characterized in that the mixture comprising ethyl cellulose, polycaprolactone and collagen is subjected to electrospinning (106) at a voltage value of 36 kV.
13. An artificial blood vessel production method according to claim 1 , characterized in that the mixture containing ethyl cellulose, polycaprolactone and collagen is subjected to electrospinning procedure for a period of 3 to 5 hours (106).
14. An artificial blood vessel production method according to claim 14 , characterized in that the mixture containing ethyl cellulose, polycaprolactone and collagen is subjected to electrospinning procedure for a period of 4 hours.
15. An artificial blood vessel production method according to claim 1 , characterized in that the the electrospinning procedure (106) is carried out with a cylindrical structured collector having a diameter of 0.5 cm.
16. An artificial blood vessel production method according to claim 1 , characterized in that the artificial blood vessel is obtained (108) by drying the nanocomposite structure at an oven temperature of 23 to 50° C.
17. An artificial blood vessel production method according to claim 16 , characterized in that the step of obtaining the artificial blood vessel (108) by drying the nano composite scaffold in an oven is performed at 35° C.
18. An artificial blood vessel production method according to claim 16 , characterized in that the step of obtaining artificial blood vessel (108) is performed by drying the nano composite scaffold in the oven for 3 to 8 hours.
19. An artificial blood vessel production method according to claim 18 , characterized in that the step (108) of obtaining the artificial blood vessel is performed by drying the nano composite scaffold for 4 hours in the oven.
20. A biomimetic artificial blood vessel comprising ethyl cellulose, polycaprolactone and collagen obtained by a method according to claim 1 .
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TR2017/07216 | 2017-05-16 | ||
TR2017/07216A TR201707216A2 (en) | 2017-05-16 | 2017-05-16 | BIOMIMETIC AN ARTIFICIAL BLOOD VESSEL AND ITS PRODUCTION METHOD |
PCT/TR2018/050240 WO2019032069A2 (en) | 2017-05-16 | 2018-05-16 | A biomimetic artificial blood vessel and a production method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
US20200061247A1 true US20200061247A1 (en) | 2020-02-27 |
Family
ID=65272487
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US16/612,677 Pending US20200061247A1 (en) | 2017-05-16 | 2018-05-16 | A biomimetic artificial blood vessel and a production method thereof |
Country Status (4)
Country | Link |
---|---|
US (1) | US20200061247A1 (en) |
EP (1) | EP3628013B1 (en) |
TR (1) | TR201707216A2 (en) |
WO (1) | WO2019032069A2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111603267A (en) * | 2020-06-12 | 2020-09-01 | 西安交通大学医学院第一附属医院 | Method for manufacturing coaxial electrostatic spinning magnetic anastomosis artificial blood vessel |
CN113017913A (en) * | 2021-04-15 | 2021-06-25 | 四川大学华西医院 | Absorbable artificial blood vessel and preparation method thereof |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113046917B (en) * | 2021-02-07 | 2022-10-21 | 西华师范大学 | Electrostatic spinning collagen membrane and preparation method thereof |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101385872A (en) * | 2008-10-24 | 2009-03-18 | 东华大学 | Method for preparing absorbable biological material artificial blood vessel bracket using electro-spinning |
US20100221304A1 (en) * | 2009-02-26 | 2010-09-02 | The Regents Of The University Of Colorado, A Body Corporate | Bionanocomposite Materials and Methods For Producing and Using the Same |
WO2013059780A1 (en) * | 2011-10-21 | 2013-04-25 | Nitta Casings Inc. | Collagen-polysaccharide materials mimicking blood vessels, tissues and bones for medical, pharmaceutical and orthopedic applications, and processes for producing the same |
CN104562438B (en) * | 2013-10-17 | 2017-07-14 | 中国科学院理化技术研究所 | Gelatin-based micro nanometer fiber membrane material and its production and use |
US10092679B2 (en) * | 2013-10-18 | 2018-10-09 | Wake Forest University Health Sciences | Laminous vascular constructs combining cell sheet engineering and electrospinning technologies |
US20150273119A1 (en) * | 2014-03-26 | 2015-10-01 | Snu R&Db Foundation | Formulation comprising anti-scarring agents and biocompatible polymers for medical device coating |
CN105079874A (en) * | 2014-05-14 | 2015-11-25 | 复旦大学附属华山医院 | Method for preparing small-diameter artificial blood vessels on basis of nanotechnologies |
CN105983134A (en) * | 2015-03-05 | 2016-10-05 | 刘畅 | Artificial blood vessel and preparation method thereof |
-
2017
- 2017-05-16 TR TR2017/07216A patent/TR201707216A2/en unknown
-
2018
- 2018-05-16 WO PCT/TR2018/050240 patent/WO2019032069A2/en unknown
- 2018-05-16 EP EP18844923.5A patent/EP3628013B1/en active Active
- 2018-05-16 US US16/612,677 patent/US20200061247A1/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111603267A (en) * | 2020-06-12 | 2020-09-01 | 西安交通大学医学院第一附属医院 | Method for manufacturing coaxial electrostatic spinning magnetic anastomosis artificial blood vessel |
CN113017913A (en) * | 2021-04-15 | 2021-06-25 | 四川大学华西医院 | Absorbable artificial blood vessel and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
EP3628013B1 (en) | 2023-07-12 |
TR201707216A2 (en) | 2018-12-21 |
EP3628013A4 (en) | 2021-04-21 |
EP3628013C0 (en) | 2023-07-12 |
WO2019032069A2 (en) | 2019-02-14 |
EP3628013A2 (en) | 2020-04-01 |
WO2019032069A3 (en) | 2019-05-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Zhao et al. | Application of conductive PPy/SF composite scaffold and electrical stimulation for neural tissue engineering | |
Tan et al. | Composite vascular grafts with high cell infiltration by co-electrospinning | |
DE69828050T2 (en) | A process for producing a polyvinyl alcohol cryogel | |
EP3351376B1 (en) | Silk biomaterials and methods of use thereof | |
Yoo et al. | Augmented peripheral nerve regeneration through elastic nerve guidance conduits prepared using a porous PLCL membrane with a 3D printed collagen hydrogel | |
EP3628013B1 (en) | A biomimetic artificial blood vessel and a production method thereof | |
Nseir et al. | Biodegradable scaffold fabricated of electrospun albumin fibers: mechanical and biological characterization | |
CN107574497B (en) | Electrostatic spinning fiber modified composite membrane and preparation method thereof | |
Zhai et al. | Coaxial electrospinning of P (LLA‐CL)/heparin biodegradable polymer nanofibers: Potential vascular graft for substitution of femoral artery | |
Tavakoli et al. | Coaxial electrospun angiogenic nanofiber wound dressing containing advanced platelet rich-fibrin | |
CN107823692A (en) | A kind of wound dressing composite nano-fiber membrane and preparation method thereof | |
KR101604584B1 (en) | Composite comprising hydroxyapatite, chitosan or its derivative, and catechol or its derivative and use thereof | |
Hajiali et al. | Influence of topography of nanofibrous scaffolds on functionality of engineered neural tissue | |
CN112107728A (en) | Antibacterial peptide beta-HBD-3 loaded PCL/Zif-8 tissue engineering scaffold material and preparation method thereof | |
Nasonova et al. | Biocompatibility and structural features of biodegradable polymer scaffolds | |
Mao et al. | Nerve ECM and PLA-PCL based electrospun bilayer nerve conduit for nerve regeneration | |
Wang et al. | Electrospun, reinforcing network-containing, silk fibroin-based nerve guidance conduits for peripheral nerve repair | |
CN104287869B (en) | A kind of novel nano tunica fibrosa/yarn count frame for graft of trachea and preparation method thereof | |
CN113046917B (en) | Electrostatic spinning collagen membrane and preparation method thereof | |
Ghorbani et al. | Evaluation of nanofiber PLA scaffolds using dry-and wet-electro spinning methods | |
Nie et al. | PBAT/gelatin hybrid nanofibers based on post-double network bond processing as a promising vascular substitute | |
US20230374299A1 (en) | Development and Characterization of F-Gelatin Electrospun Scaffolds for Cardiac Tissue Modeling | |
Majidnia et al. | The Effect of Aligned and Random PCL-Human Amniotic Membrane Powder Scaffolds on Retinal Tissue Engineering | |
Minghui et al. | Tines made of degradable materials with decreasing removal forces: An option to facilitate passive-fixation leads extraction from the very beginning? | |
TWI582279B (en) | A core-resistant nanofiber film having anti-sticking and a method for producing the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STPP | Information on status: patent application and granting procedure in general |
Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: NON FINAL ACTION MAILED |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER |
|
STPP | Information on status: patent application and granting procedure in general |
Free format text: NOTICE OF ALLOWANCE MAILED -- APPLICATION RECEIVED IN OFFICE OF PUBLICATIONS |